Inhibition of AXL signaling in anti-metastatic therapy

Patent metadata

Field	Value
Publication number	US-9266947-B2
Application number	US-201313950111-A
Country	US
Kind code	B2
Filing date	Jul 24, 2013
Priority date	Jan 22, 2010
Publication date	Feb 23, 2016
Grant date	Feb 23, 2016

Abstract

Compositions and methods are provided for alleviating cancer in a mammal by administering a therapeutic dose of a pharmaceutical composition that inhibits activity of AXL protein activity, for example by competitive or non-competitive inhibition of the binding interaction between AXL and its ligand GAS6.

First claim

The invention claimed is:

1. A method of inhibiting growth, metastasis or invasion of a tumor that expresses Axl or GAS6 in a human patient, the method comprising:
administering to said patient an effective dose of an isolated soluble AXL variant polypeptide, wherein said polypeptide lacks the AXL transmembrane domain and has a set of amino acid substitution(s) of the wild-type AXL sequence (SEQ ID NO. 1) selected from the group consisting of 1) Gly32Ser, Asp87Gly, Val92Ala, and Gly127Arq, 2) Glu26Gly, Val79Met, Val92Ala, and Gly127Glu, 3) Asn33Ser, Ser74Asn, Asp87Gly, and Val92Ala, 4) Ala72Val, Ile97Arq, and His116Arq, 5) Gln78Glu, 6) Ala72Val, 7) Gln86Arq, Ile90Val, and Val92Ala, 8) Ala72Val, and Val92Asp, 9) Asp65Asn, and Asp87Gly, 10) Asp87Gly, and Val92Ala, 11) Glu27Lys, His61Tyr, Ala72Val, Asp88Asn, Val92Ala, and Thr98Ala, 12) Val92Ala, Gln109Arq, 13) Thr44Ala, Ala72Val, Ile90Val, Thr105Met, and Glu129Lys, 14) Val92Gly, 15) Val92Ala, Val112Ala, Phe113Leu, and Thr118Ala, 16) Val92Ala, and Thr98Pro, 17) Glu27Gly, and Asp87Gly, 18) Thr3811e, and Val92Ala, 19) Asp87Gly, 20) Thr23Met, and Val92Ala, 21) Ala72Val, and Phe113Leu, 22) Gln86Arg, Val92Ala, 23) Ala19Thr, Glu26Gly, Glu27Gly, and Val92Ala, 24) Ile90Met and Val92Ala, 25) Gly32Ser, and Asp87Gly, 26) Gly32Ser, and Val92Ala, 27) Gly32Ser, and Gly127Arg, 28) Asp87Gly, and Gly127Arg, 29) Val92Ala, and Gly127Arg, 30) Asp87Gly, Val92Ala, and Gly127Arg, 31) Gly32Ser, Val92Ala, and Gly127Arg, 32) Gly32Ser, Asp87Gly, and Gly127Arg, 33) Gly32Ser, Asp87Gly, and Val92Ala and 34) Gly32Ser, Ala72Val, Asp87Gly, Val92Ala, and Gly127Arg; in a dose effective to inhibit growth, metastasis or invasion of the tumor that expresses Axl or GAS6.

2. A method of inhibiting growth, metastasis or invasion of a tumor that expresses Axl or GAS6 in a human patient, the method comprising:
administering an isolated soluble AXL variant polypeptide, wherein said polypeptide lacks the AXL transmembrane domain and has an amino acid substitution at position 32, 72, 87, 92, or 127 of the wild-type AXL sequence (SEQ ID NO: 1) or a combination thereof and wherein said polypeptide binds to GAS6 with a binding affinity that is higher than the binding affinity of the wild-type AXL to GAS6; in a dose effective to inhibit growth, metastasis or invasion of the tumor that expresses Axl or GAS6.

3. The method of claim 1 , wherein the Axl variant polypeptide is a fusion protein comprising an Fc domain.

4. The method of claim 2 , wherein the Axl variant polypeptide is a fusion protein comprising an Fc domain.

5. The method of claim 1 , further comprising administering at least one cytotoxic agent to said patient.

6. The method of claim 2 , further comprising administering at least one cytotoxic agent to said patient.

Assignees

• Univ Leland Stanford Junior

Inventors

• Giaccia Amato J
• Rankin Erinn Bruno
• Cochran Jennifer R
• Jones Douglas
• Kariolis Mihalis
• Fuh Katherine
• Miao Yu

Classifications

• A61P35/04

  specific for metastasis · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• C07K14/705 Primary

  Receptors; Cell surface antigens; Cell surface determinants {(tumour specific antigens C07K14/4748)} · CPC title

• C07K2319/30

  Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto · CPC title

• A61K38/00

  Medicinal preparations containing peptides (peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00) · CPC title